Variant report

Variant	rs367593507
Chromosome Location	chr8:126632029-126632030
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6377	chr8:126579620-126639253	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv38	chr8:126593465-126639253	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3480615	chr8:126631554-126632034	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv3492925	chr8:126631577-126632089	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3492926	chr8:126631621-126632063	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126627200-126633400	Weak transcription	Adipose Nuclei	Adipose
2	chr8:126627800-126632200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr8:126628000-126632200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr8:126628800-126649400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:126632000-126635200	Enhancers	Primary monocytes fromperipheralblood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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